Christine Hunter

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Christine Hunter is the mother of Alison Hunter, a teen who died following complications from a severe case of myalgic encephalomyelitis (ME). In her honor, Ms. Hunter chaired the Australia’s Alison Hunter Foundation established in 1998 to foster research for ME until it merged in 2014 with the National Centre for Neuroimmunology and Emerging Diseases (N.C.N.E.D.) at Griffith University, Queensland.[1]

Christine Hunter also carried on her daughter's legacy by chairing the MEYA/ ME Young Adults, a group her daughter started in 1992 for young adults with ME for awareness and support.[2]

Awards[edit | edit source]

  • 2004, IACFS/ME Special Service Award - for outstanding personal effort and contribution to the CFS/ME community (She shared the award with Judy Basso)[3]</ref>

Talks and interviews[edit | edit source]

See also[edit | edit source]

References[edit | edit source]

myalgic encephalomyelitis (ME) - A disease often marked by neurological symptoms, but fatigue is sometimes a symptom as well. Some diagnostic criteria distinguish it from chronic fatigue syndrome, while other diagnostic criteria consider it to be a synonym for chronic fatigue syndrome. A defining characteristic of ME is post-exertional malaise (PEM), or post-exertional neuroimmune exhaustion (PENE), which is a notable exacerbation of symptoms brought on by small exertions. PEM can last for days or weeks. Symptoms can include cognitive impairments, muscle pain (myalgia), trouble remaining upright (orthostatic intolerance), sleep abnormalities, and gastro-intestinal impairments, among others. An estimated 25% of those suffering from ME are housebound or bedbound. The World Health Organization (WHO) classifies ME as a neurological disease.

The information provided at this site is not intended to diagnose or treat any illness.
From MEpedia, a crowd-sourced encyclopedia of ME and CFS science and history.